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FDA 510(k)

Intellijoint HIP Generation 2B System

K-Number: K171525 · 2017-10-30

ApplicantIntellijoint Surgical, Inc.
Decision Date2017-10-30
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Intellijoint HIP Generation 2B System is a medical device manufactured by Intellijoint Surgical, Inc.. It received FDA 510(k) clearance on 2017-10-30 under approval number K171525. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Intellijoint HIP Generation 2B System?

Intellijoint HIP Generation 2B System is a medical device that received FDA 510(k) clearance on 2017-10-30. It is manufactured by Intellijoint Surgical, Inc.. The 510(k) number is K171525.

When was Intellijoint HIP Generation 2B System approved by the FDA?

Intellijoint HIP Generation 2B System received FDA 510(k) clearance on 2017-10-30, under approval number K171525.

What company makes Intellijoint HIP Generation 2B System?

Intellijoint HIP Generation 2B System is manufactured by Intellijoint Surgical, Inc..

What is the FDA product code for Intellijoint HIP Generation 2B System?

The FDA product code for Intellijoint HIP Generation 2B System is OLO.

Related Clinical Trials

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Other Devices by Intellijoint Surgical, Inc.

K172849Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray K162364Intellijoint HIP Generation 2A System K191507Intellijoint® Navigation System K211876Intellijoint VIEW

Related Devices (Code: OLO)

K162375Envision 3D: Image Guidance System7D Surgical, Inc. K162341Stryker OrthoMap Precision Knee systemStryker Leibinger GmbH & Co KG K162195TSolution One Cup1 Surgical SystemTHINK Surgical, Inc. K160385Precision ScrewCryptych Pty, Ltd. K153700Aesculap(R) Implant Systems (AIS) S4 Navigation InstrumentsAesculap Implant Systems, LLC K153240Styrker OrthoMap Express Knee SystemStryker Corporate

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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